関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl 2-methylacetoacetate | HCID 701 | — |
| 反応物 | Boron trifluoride etherate | HCID 8000 | — |
| 反応物 | 4-Tert-butyl-2-fluoroaniline | HCID 10464690 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | HCID 178432297 | HCID 178432297 | 23.4% |
反応手順
4-t-Butyl-2-fluoroaniline (4.79 g) prepared according to the above process and ethyl 2-methyl-acetoacetate (4.96 g) were refluxed in toluene (60 ml) in the presence of trifluoroboron etherate (0.3 ml) for 3 hr to obtain a reaction solution. The reaction solution thus obtained was washed with a saturated aqueous sodium hydrogencarbonate solution and saturated brine and was dried over anhydrous sodium sulfate. The solvent was then removed under the reduced pressure. The reaction product was refluxed in diphenyl ether (80 ml) for one hr and was allowed to stand for cooling. The precipitated product was then collected by filtration under the reduced pressure to give 2,3-dimethyl-6-t-butyl-8-fluoro-4-hydroxyquinoline (compound 1, 1.66 g). 1H-NMR data on this compound in deutro-DMSO (dimethyl sulfoxide) were as shown below.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06787557B2 |
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| 出典データセット | uspto-grants-2004_09 |
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| ORD ID | ord-9f0d6bcbf76641629e3a04a844e35a09 |
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| 出典メモ | uspto-grants-2004_09 |
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